Canonical Allele Identifier: CA129534355
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs956790979
MyVariant Identifiers: chr5:g.145038756C>G (hg19) chr5:g.145659193C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659193C>G , CM000667.2:g.145659193C>G GRCh38
NC_000005.9:g.145038756C>G , CM000667.1:g.145038756C>G GRCh37
NC_000005.8:g.145018949C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105738G>C
XR_944308.1:n.662+105738G>C
XM_017009130.1:c.*6163G>C XP_016864619.1:n.*6163G>C
XM_017009133.1:c.*6195G>C XP_016864622.1:n.*6195G>C
XR_001742025.1:n.913+44782G>C
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